Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

por Marco, Elysa Jill, Aitken, Anne Brandes, Nair, Vishnu Prakas, da Gente, Gilberto, Gerdes, Molly Rae, Bologlu, Leyla, Thomas, Sean, Sherr, Elliott H.
Publicado 2018

Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region

por Moufawad El Achkar, Christelle, Rosen, Alyssa, Kessler, Sudha Kilaru, Steinman, Kyle J., Spence, Sarah J., Ramocki, Melissa, Marco, Elysa Jill, Green Snyder, LeeAnne, Spiro, John E., Chung, Wendy K., Annapurna, Poduri, Sherr, Elliott H.
Publicado 2022